Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K190373 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment is suitable for radiographic and ... | 2 | 11/07/2024 |
FEI # 3002808139 SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION |
| MODEL: X-RAY TV SYSSTEM SONIALVISION safire17 | 2 | 04/07/2022 |
FEI # 1000125362 Shimadzu Medical Systems |
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